Evidence map›Paper›PMID 26477596›Full record

ReviewJournal of internal medicine2015

The small leucine-rich repeat proteoglycans in tissue repair and atherosclerosis.

A Hultgårdh-Nilsson, J Borén, S Chakravarti

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of internal medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 74 citations in OpenAlex.

  1. Trial
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  11. Vascular Extracellular Matrix in Atherosclerosis.International journal of molecular sciences · 2024
    Review
  12. Review
  13. The role of CD8Heliyon · 2024
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 2 countries.

A Hultgårdh-NilssonDepartment of Experimental Medical Science, Lund University, Lund, Sweden.
J BorénDepartment of Molecular and Clinical Medicine/Wallenberg Laboratory, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.
S ChakravartiDepartments of Medicine, Ophthalmology and Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Johns Hopkins Medicine · USLund University · SEUniversity of Gothenburg · SE

Funding

The Role of Lumican in the CorneaR01EY011654 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHAKRAVARTI, SHUKTI · 1997 to 2017
$6.1M
The Role of Lumican in the corneaR56EY011654 · NEI · JOHNS HOPKINS UNIVERSITY · PI CHAKRAVARTI, SHUKTI · 2007 to 2007
$474k
NEI NIH HHS EY11654NEI NIH HHS R01 EY011654NEI NIH HHS R56 EY011654
6 · The paper itself

Abstract

Proteoglycans consist of a protein core with one or more covalently attached glycosaminoglycan (GAG) side chains and have multiple roles in the initiation and progression of atherosclerosis. Here we discuss the potential and known functions of a group of small leucine-rich repeat proteoglycans (SLRPs) in atherosclerosis. We focus on five SLRPs, decorin, biglycan, lumican, fibromodulin and PRELP, because these have been detected in atherosclerotic plaques or demonstrated to have a role in animal models of atherosclerosis. Decorin and biglycan are modified post-translationally by substitution with chondroitin/dermatan sulphate GAGs, whereas lumican, fibromodulin and PRELP have keratan sulphate side chains, and the core proteins have leucine-rich repeat (LRR) motifs that are characteristic of the LRR superfamily. The chondroitin/dermatan sulphate GAG side chains have been implicated in lipid retention in atherosclerosis. The core proteins are discussed here in the context of (i) interactions with collagens and their implications in tissue integrity, fibrosis and wound repair and (ii) interactions with growth factors, cytokines, pathogen-associated molecular patterns and cell surface receptors that impact normal physiology and disease processes such as inflammation, innate immune responses and wound healing (i.e. processes that are all important in plaque development and progression). Thus, studies of these SLRPs in the context of wound healing are providing clues about their functions in early stages of atherosclerosis to plaque vulnerability and cardiovascular disease at later stages. Understanding of signal transduction pathways regulated by the core protein interactions is leading to novel roles and therapeutic potential for these proteins in wound repair and atherosclerosis.

Indexed as

ProteinsAnimalsAtherosclerosisChondroitin Sulfate ProteoglycansHumansLeucine-Rich Repeat ProteinsRepetitive Sequences, Amino AcidSignal TransductionWound HealingChondroitin Sulfate ProteoglycansLeucine-Rich Repeat ProteinsProteinsatherosclerosisbiglycandecorinfibromodulinlumicansmall leucine-rich repeat proteoglycan

Identifiers

PMID26477596
PMCPMC4616156
OpenAlexW2122486924

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.